CHEBI:78322 - ethyl (2S)-lactate

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ChEBI Name ethyl (2S)-lactate
ChEBI ID CHEBI:78322
ChEBI ASCII Name ethyl (2S)-lactate
Definition The (2S)-enantiomer of ethyl lactate.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C5H10O3
Net Charge 0
Average Mass 118.13110
Monoisotopic Mass 118.06299
InChI InChI=1S/C5H10O3/c1-3-8-5(7)4(2)6/h4,6H,3H2,1-2H3/t4-/m0/s1
InChIKey LZCLXQDLBQLTDK-BYPYZUCNSA-N
SMILES CCOC(=O)[C@H](C)O
Roles Classification
Biological Role(s): Saccharomyces cerevisiae metabolite
Any fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae ).
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
(via ethyl 2-hydroxypropanoate )
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ChEBI Ontology
Outgoing ethyl (2S)-lactate (CHEBI:78322) has role Saccharomyces cerevisiae metabolite (CHEBI:75772)
ethyl (2S)-lactate (CHEBI:78322) is a ethyl 2-hydroxypropanoate (CHEBI:78321)
ethyl (2S)-lactate (CHEBI:78322) is enantiomer of ethyl (2R)-lactate (CHEBI:78323)
Incoming rac-ethyl lactate (CHEBI:78319) has part ethyl (2S)-lactate (CHEBI:78322)
ethyl (2R)-lactate (CHEBI:78323) is enantiomer of ethyl (2S)-lactate (CHEBI:78322)
IUPAC Name
ethyl (2S)-2-hydroxypropanoate
Synonyms Sources
(L)-(−)-ethyl lactate ChemIDplus
(L)-ethyl lactate ChemIDplus
Manual Xref Database
Ethyl_lactate Wikipedia
View more database links
Registry Numbers Types Sources
1720839 Reaxys Registry Number Reaxys
687-47-8 CAS Registry Number ChemIDplus
Last Modified
23 April 2014